Musa - Science topic

In this case, quite a number of pigments are more temperature-stable than dyes. so just like Robert Bernard Pansu mentioned, you can select a pigment and try modifying it to suit your need. sulfonate and/or few hydroxyl groups should save the day.

alternatively, you can try out disperse dyes (depending on the area of application) because they are designed for dyeing wholly synthetic fibres in high temperature dyeing.

i hope this helps

Roberto Carlos Soto Glyphosate can be washed into soil and be absorbed by banana roots.

See: Saunders, Lyndsay E., and Reza Pezeshki. "Glyphosate in runoff waters and in the root-zone: a review." Toxics 3.4 (2015): 462-480.

It seems like you are trying to compare a DFT optimized structure with the crystal structure. I think 'ORTEP' should work for the same.

Look, please, to Paulo Pereira's from Mykolas Romeris university, Vilnius, Lithuania, publications.

Almost all modern edible seedless (parthenocarp) bananas come from two wild species – Musa acuminata and Musa balbisiana. The scientific names of most cultivated bananas are Musa acuminata, Musa balbisiana, and Musa × paradisiaca for the hybrid Musa acuminata × M. balbisiana, depending on their genomic constitution. The old scientific name for this hybrid, Musa sapientum, is no longer used.

If he/she is telling true yes

Dear Finsbury Trogun,

Please, look at these articles. I hope they will be of interest for you.

Best regards,

Check on this paper.

For crude lipid/fat, Sohxlet would be better choice. Whereas, use a combination of organic solvents for the estimation of total lipids.

Answer was send on the las 23 March with several recommendadionts according the Musa spp. genome .

You will see it is working, successes.

Hi Anand Mohan

Kindly let me know, which locus/regions did you sequenced? ITS? SSU? LSU? or?

your fungal isolate is an endophyte and it didn't produced spores in PDA medium based on your information. I have observed rare occurrence of asexual sporulation in laboratory culture. Most isolates, however, have not been observed to sporulate in laboratory culture. Due to the absence of morphological characters as a key for sorting isolates, some researchers have used methods such as restriction enzyme digests (e.g. RFLPs) of the ITS region to assess the degree of relatedness between sporulating and nonsporulating isolates. Very few studies have characterized isolates with a DNA sequencing-based approach. Sequence information not only allows opportunities for easy comparison of isolates from other studies, but also allows researchers to assess the phylogenetic positions of these organisms.

My suggestion is, you can try some other medium which can induce sporulation or try to sequence other more conserved regions such as: translation elongation factor 1-α, β-tubulin, and actin genes, and analysis of secondary metabolites.

I hope this would helps you

Goodluck!

Thank you So Much Dr Ajit Arun Waman for your suggestions and answer.

Thank you @ Jesús María Vielba .if possible any hands on workshop pls let me know..

As temperature increased, the dry weight of the roots decreased. In this experiment , leaf width decreased at 38 degree C and 43 degree C. At 43 degree C, roots were brown and suberized and lacked root tips. Lack of roots tips may affect the hormone balance of the plant and thus the distribution of photosynthates.

Sir, I am not from animal science, Thanks

Subir Bandyopadhyay Sir, Thanks for your precious response.

Aspidiotus is a genus of armored-scale insects that cause severe damage by piercing and sucking their host crops. They reproduce sexually by producing eggs that hatch into crawlers and crowlers that develop into sedentary adults. Their life cycles are typically around one month and their only mobile stage is the crawler stage. They prefer perennial than annual crops because perennial crops provide continuous source of food without a need for the crawlers to travel long distance once they have established. 

Root crops have modified roots to function as storage organs, while tuber crops have modified stems or roots to function as both storage and propagation organs. As such, the modified roots of root crops cannot propagate new crops, whereas the modified stem or roots of tuber crops can propagate new crops. Examples of root crops are potato, sweet potato, and dahlia; examples of tuber crops are carrot, sugar beet, and parsnip.

Hope this will help: http://www.batcon.org/resources/media-education/bats-magazine/bat_article/1033?tmpl=component

5G New Radio is primarily using multi-user MIMO (also known as Massive MIMO) for multiple access.

I know that there is a lot of research into other multiple access methods. Maybe some of them will eventually be used in situations where multi-user MIMO is insufficient, but I think far from that point. As an example, NOMA is useful when you have few antennas, but most 5G base stations will probably have many antennas.

Hi!

An answer more from personal experience than from science, maybe: I am sure you are right when writing that "a lot of factors come in".

To experience correction and criticism on pronounciation is like when parents too ambitiously overcorrect their toddlers when learning to speak the first language, the mother tongue.

Children must be given time and opportunity to gradually find out the right pronounciation for themselves for becoming understood. Consequences can otherwise become problems as stuttering and stammering; troublesome personal communication filled with anxiety to get it right and normal - and it becomes wrong and not normal, all the time. Very personal and damaging. I know.

Now, L2 learning is of course not all like L1 learning, but I think teachers should have a lot of patience here when pupils try to express themselves in another langugage, Respect what they are trying to communicate instead of correcting their way of doing it. It is about personality and about being accepted as anyone else - and for what you say, not the way of saying it. The more they try to really communicate in a second language, and ideally with native speakers, the more they will adapt to better pronounciation. Let them think enhancement was their own idea. Only help them technically with producting a special sound etc - but as a group activity, preferably. Communication ability is a serious and very personal thing.

Upon reading your question, my first instinct is that you may be seeing that your primers are binding not just to where you expect, but also binding with one or more mismatches to another genomic region. It sounds like some troubleshooting should be done so that you can eliminate mis-priming as a confounding factor.

A few simple experiments: 1) raise your hybridization temperature by a few degrees, since higher temperature will disrupt imperfect pairing in 'mis-priming' events. This will normally reduce yield of the expected target, so you might add more cycles to offset. 2) move both primers in or out, so that they have difference sequences, and perhaps you will eliminate any 'mis-priming' events. 3) nested PCR: amplifying with a second set of primers using your first amplicon as the template. In this case, 4 primers give better target sequence specificity than only 2 primers.

Hi there, 

I would like to ask about the calculation of the Trolox Equivalent. I had the standard curve, but I am stuck in how to calculate the TE of the sample.

Many thanks,

try to supplement your current media formulation (that have PGRs) with about 20 - 100ng/L of polyamine (putrescine) in the media. this is likely to enhance multiplication at all stage

There are a lot published literature for banana in vitro propagation.you can use the simple MS medium with BAP as cytokinin in a concentration of 1 to 5 mg/L and auxin at at 1 mg/l.